Single active layer electrochromic devices

ABSTRACT

In one embodiment, an electrochromic device includes a single active layer configured to be alternately placed in a light-transmitting state in which relatively large amounts of light can be transmitted through the active layer and a light-blocking state in which relatively small amounts of light can be transmitted through the active layer, wherein the device comprises no other layers of material that contribute to transitioning between the two states.

CROSS-REFERENCE TO RELATED APPLICATION

This application is the 35 U.S.C. § 371 national stage application of PCT Application No. PCT/2018/032914, filed May 16, 2018, where the PCT claims priority to U.S. Provisional Application Ser. No. 62/507,359, filed May 17, 2017, both of which are herein incorporated by reference in their entireties.

BACKGROUND

Electrochromic devices are devices whose optical properties, such as light transmission and absorption, can be altered in a reversible manner through the application of a voltage. This property enables electrochromic devices to be used in various applications, such as smart windows, electrochromic mirrors, and electrochromic display devices.

Most commercially available electrochromic devices are relatively complex devices that comprise multiple layers of different materials that are required for the device to change state. As an example, some electrochromic devices comprise a layer of conductive glass, a layer of a metal oxide, an electrochromic layer, an ionic electrolyte layer, and a further layer of conductive glass. When an electrical potential is applied to such a device, an electrochemical reaction occurs at the interface of the two active layers (i.e., the electrochromic layer and the electrolyte layer), which changes the redox state of a polymer contained in the electrochromic layer, thereby changing the color of the electrochromic layer. In addition to their complexity, such devices can require expensive processes, materials, or equipment to manufacture. In view of this, it would be desirable to have simpler electrochromic devices that are less expensive to manufacture.

BRIEF DESCRIPTION OF THE DRAWINGS

The present disclosure may be better understood with reference to the following figures. Matching reference numerals designate corresponding parts throughout the figures, which are not necessarily drawn to scale.

FIGS. 1A and 1B are schematic views of an embodiment of an electrochromic device showing the device in a light-blocking state and a light-transmitting state, respectively.

FIGS. 2A and 2B are photographs of a fabricated electrochromic device having a single polyvinyl alcohol (PVA)+ammonium perdisulphate (APS)+methylene blue (MB)+polyaniline (PANI) active layer shown in a light-blocking state and a light-transmitting state, respectively.

FIGS. 3A-3C are scanning electron microscope (SEM) images of PVA+APS+MB, PVA+APS+PANI, and PVA+APS+MB+PANI active layers, respectively.

FIG. 4 is a graph that shows Fourier-transform infrared spectroscopy (FTIR) transmission peaks for a PVA+APS active layer.

FIG. 5 is a graph that shows UV-vis optical absorption for various active layers.

FIG. 6A is a graph that shows cyclic voltammetries (CVs) of a PVA+APS+MB device as a function of scan rate.

FIG. 6B is a graph that shows CVs of a PVA+APS+PANI device as a function of scan rate.

FIG. 6C is a graph that shows CVs of a PVA+APS+PANI+MB device as a function of scan rate.

FIGS. 7A-7D are graphs that show CVs of PVA+APS+PANI+MB devices at 50 mV/sec where the active layer is formed by keeping molar ratios of aniline to methylene blue at 1:2.0, 1:2.5, 1:3, and 1:5, respectively.

FIGS. 8A-8C are graphs that show chronoamperometric results for PVA+APS+PANI, PVA+APS+MB, and PVA+APS+MB+PANI devices.

FIG. 9 is a diagram that illustrates the gelling process of polyvinyl alcohol in hydrogen chloride.

FIG. 10 is a diagram that illustrates the gelling process of polyvinyl alcohol in hydrogen chloride with ammonium persulfate as an oxidant.

FIG. 11 is a diagram that illustrates the formation of emeraldine salt in the presence of hydrogen chloride and ammonium persulfate after polymerization of aniline to emeraldine salt.

FIG. 12 is a diagram that illustrates emeraldine salt changing to pernigraniline due to presence of ammonium persulfate and oxidized polyvinyl alcohol in ammonium persulfate.

FIG. 13 is a diagram that illustrates coloration and decoloration due to the application of a voltage across a single PVA+HCl+APS+MB+PANI active layer.

DETAILED DESCRIPTION

As described above, it would be desirable to have electrochromic devices that are relatively simple in construction and that are relatively inexpensive to manufacture. Disclosed herein are examples of such devices. The electrochromic devices comprise a single active layer that can be transitioned from a light-transmitting state, in which a relatively large amount of light can be transmitted through the device, to a light-blocking state, in which a relatively small amount of light can be transmitted through the device, by controlling the electrical potential applied across the active layer. For example, the light-blocking state can be achieved when an electrical potential is applied to the active layer and the light-transmitting state can be achieved by reversing the electrical potential. In some embodiments, the active layer comprises a base polymer that includes an acid and an oxidant as well as a conducting polymer, a dye, or both. The active layer can be sandwiched between opposed transparent or translucent layers of material, such as glass, that protect the active layer and form a complete electrochromic “window.”

In the following disclosure, various specific embodiments are described. It is to be understood that those embodiments are example implementations of the disclosed inventions and that alternative embodiments are possible. All such embodiments are intended to fall within the scope of this disclosure.

FIGS. 1A and 1B illustrate an example electrochromic device 10 in accordance with this disclosure. It is noted that the electrochromic devices disclosed herein, including the device 10, can be used as is or can be incorporated into other objects. For example, the disclosed electrochromic devices can be used as or incorporated into windows that can be alternately placed in a first state in which they block or absorb light and a second state in which they freely transmit light, depending on the desired effect.

As used herein, phrases such as “blocking” or “absorbing” light, or “reducing” or “limiting” the amount of light that can pass are not intended to be limited to situations in which no light can pass through the electrochromic device. Accordingly, when an electrochromic device is described herein as blocking, absorbing, reducing, limiting, etc. light or light transmission, the device may still enable some light to pass. In similar manner, phrases such as “transmitting” light or “enabling” light to pass are not intended to be limited to situations in which all light can pass through the electrochromic device without any light being blocked or absorbed. Accordingly, an electrochromic device that transmits light, enables light to pass, etc. may block or absorb some light and does not necessarily need to be completely transparent. Generally speaking then, the electrochromic devices disclosed herein can be described as having a first state in which relatively low amounts of light can pass and a second state in which relatively high amounts of light can pass.

With reference to FIGS. 1A and 1B, the electrochromic device 10 generally comprises a single active layer of material, or “active layer,” 12 that is positioned (e.g., sandwiched) between first and second transparent or translucent layers of material, or “layers,” 14 and 16. The active layer 12 is considered to be “active” because it is required to obtain a change in state. This is in contrast to the transparent or translucent layers 14, 16 that are not required to obtain the state change (and therefore are not active layers) but are instead provided to protect the active layer 12 and form a complete electrochromic window. Accordingly, there are no layers of the device 10 other than the single active layer 12 that contribute to the state change of the device.

In some embodiments, the layers 14, 16 comprise thin transparent glass or plastic plates that are coated with a transparent, electrically conductive film 18, 20 that facilitates the application of electrical potentials to the active layer 12. The transparent, electrically conductive films 18, 20 can, in some embodiments, comprise a transparent conducting oxide (TCO), such as indium tin oxide (ITO), fluorine doped tin oxide (FTO), or doped zinc oxide (ZnO). Irrespective of the composition of the transparent, electrically conductive films 18, 20, the films at least cover the surfaces of the layers 14, 16 that face the active layer 12.

The active layer 12 comprises one or more base polymers that form a conducting matrix. In some embodiments, the base polymer comprises one or more water-soluble, synthetic polymers. Example water-soluble, synthetic polymers include polyvinyl alcohol (PVA), poly (vinyl acetate), poly (vinyl alcohol co-vinyl acetate), polyvinyl acetate-vinyl alcohol, poly (methyl methacrylate, poly (vinyl alcohol-co-ethylene ethylene), poly (vinyl butyral-co-vinyl alcohol-co-vinyl acetate), poly(vinyl alcohol)-acrylamide, polyvinyl butyral, polyvinyl chloride, poly(vinyl nitrate), substituted (butyryl, palmitic, capryloyl, lauric, myristic, and stearic acids, myristol, halogens, azide, or amines, poly(vinyl alcohol), carboxylated poly(vinyl alcohol), poly(vinyl chloride-co-vinyl acetate-co-vinyl alcohol), poly(vinyl acetate-co-acrylic acid), poly(vinyl alcohol-co-acrylic acid), poly(vinyl alcohol)-acrylamide, poly(vinyl alcohol)-salicylic acid, poly(vinyl methyl ketone), polyacrylamides, polyamines, polyvinylpyrrolidone, and mixtures thereof.

The base polymer is mixed with one or more acids to form an electrolytic composition. Example acids include glacial acetic acid (CH₃COOH), propionic acid (C₃H₆O₂), hydrochloric acid (HCl), hydrofluoric acid (HF), phosphoric acid (H₃PO₄), acetic acid (non-glacial) (CH₃COOH), sulfuric acid (H₂SO₄), formic acid (CH₂O₂), benzoic acid (O₇H₆O₂), nitric acid (HNO₃), phosphoric acid (H₃PO₄), sulfuric acid (H₂SO₄), tungstosilicic acid hydrate (H₄[Si(W₃O₁₀)₄].xH₂O), hydriodic acid (HI), carboxylic acids (C_(n)H_(2n+1)COOH), dicarboxylic acid (HO₂C—R—CO₂H), tricarboxylic acid (C₆H₈O₆), oxalic acid (O₂H₂O₄), hexacarboxylic acid (C₁₂H₆O₁₂), citric acid (C₆H₈O₇), tartaric acid (O₄H₆O₆), and mixtures thereof.

The base polymer is also mixed with one or more oxidants to enable the active layer 12 to be placed in an oxidized state. Example oxidants include aluminum nitrate (Al(NO₃)₃), ammonium dichromate ((NH₄)₂Cr₂O₇), ammonium perdisulphate (APS) ((NH₄)₂S₂O₈), barium nitrate (Ba(NO₃)₂), bismuth nitrate (Bi(NO₃)₃.5H₂O), calcium hypoperchlorate (Ca(ClO)₂), copper (II) nitrate (Cu(NO₃)₂), cupric nitrate (Cu(NO₃)₂), ferric nitrate (Fe(NO₃)₃), hydrogen peroxide (H₂O₂), lithium hydroxide monohydrate (LiOH), magnesium nitrate (Mg(NO₃)₂), magnesium perchlorate (Mg(ClO₄)₂), potassium chlorate (KClO₃), potassium dichromate (K₂Cr₂O₇), potassium permanganate (KMnO₄), sodium hypochlorite (NaClO), sodium periodate (NaIO₄), zinc nitrate hydrate (Zn(NO₃)₂), ammonium nitrate ((NH₄)(NO₃)), silver nitrate (AgNO₃), benzoyl peroxide (C₁₄H₁₀O₄), tetranitromethane (CN₄O₈), sodium perchlorate (NaClO₄), potassium perchlorate (KClO₄), potassium persulfate (K₂S₂O₈), sodium nitrate (NaNO₃), potassium chromate (K₂CrO₄), and mixtures thereof.

In addition to the base polymer, the acid, and the oxidant, the active layer 12 further comprises one or more colored materials. As used herein, the term “colored material” refers to a material that inherently has a color in its natural state. It is the colored material or materials that form the basis of the active layer's color when the layer is in the light-blocking state. In some embodiments, the colored material comprises one or more conducting polymers that can exist in two or more color states. When a conducting polymer is present in the active layer 12, the oxidant within the base polymer can polymerize the molecules of the conducting polymer monomers. Example conducting polymers include polyanilines (e.g., polyaniline (PANI), poly(ortho-anisidine) (POAS), poly(o-toluidine) (POT), poly(ethoxy-aniline) (POEA)), substituted polyanilines, polypyrroles, substituted polypyrroles, polythiophenes, polyindole, polycarbazole, substituted polycarbazole, polyaniline-rhodamine, polypyrrole-rhodamine, polythiophene-rhodamine, and mixtures thereof. In some embodiments, polyanilines are particularly suitable for use in the active layer 12. Polyaniline polymers can exist in a pernigraniline (violet) state, an emeraldine (blue to green) state, or a leucomeraldine (faded yellow to transparent) state.

In other embodiments, the colored material comprises one or more dyes. Example dyes include congo red, methylene blue (MB), eosin Y, methyl viologen, methyl orange, rhodamin B, crystal violet, acid fuschin, nigrosine, cationic dye, methyl orange, orange G, and mixtures thereof.

In further embodiments, the colored material comprises both one or more conducting polymers and one or more dyes. Example conducting polymers and dyes have been identified above.

Irrespective of its composition, the active layer 12 can be deposited on one of the layers 14, 16 using any one of a variety of deposition techniques, including electrochemically, by solution cast, or using a self-assembly technique.

As identified above, the active layer 12 can exist in either a light-blocking state in which relatively small amounts of (or no) light can be transmitted through the layer or a light-transmitting state in which relatively large amounts of (or all) light can be transmitted through the layer. In some embodiments, the active layer 12 is opaque or substantially opaque in the light-blocking state and transparent or substantially transparent in the light-transmitting state. In some embodiments, the active layer 12 can be in a colored state (i.e., its natural state) once the electrochromic device 10 has been fabricated prior to any electrical potential being applied. The depth (darkness) of this color depends upon the particular colored materials that are used and their concentrations within the active layer 12. When a small electrical potential is applied to the active layer 12, for example, an electrical potential greater than 0 V and up to approximately 2 V, the active layer 12 oxidizes and becomes darker (i.e., more light blocking). Significantly, when the electrical potential is removed, the active layer 12 will remain in the darker colored state (or a state close to it). Accordingly, power is not required to maintain the light-blocking state.

In order to transition the active layer into the light-transmitting state, the electrical potential that was applied to the active layer 12 is reversed such that the active layer will have little or no electrical potential. When this is achieved, the active layer 12 will be transparent (i.e., no color) or nearly transparent (i.e., a very light color). Again, no power is required to maintain this state.

The above-described color-change phenomenon is schematically illustrated in FIGS. 1A and 1B. FIG. 1A shows the electrochromic device 10 after a voltage of 1.5 V to 2.0 V has been applied to the active layer 12 using a voltage source 22. As can be seen in FIG. 1A, the active layer 12 has become substantially opaque and is, therefore, in the light-blocking state. FIG. 1B shows the device 10 after the voltage has been reversed so that the active layer 12 has 0V an electrical potential of 0V to −0.5 V. As can be appreciated from FIG. 1B, the active layer 12 is substantially transparent.

Example Embodiments

The general construction and operation of the disclosed electrochromic devices having been described above, specific examples of electrochromic devices will now be discussed.

Various active layer gels were prepared for experimentation purposes. The gels were applied between FTO-coated glass plates both with and without a physical spacer. A one nanometer to 10 μm thickness film can be formed by simply applying the gel between two FTO coated glasses with gentle pressure. Electrochromic devices comprising a thin layer of PVA+APS+MB, PVA+APS+PANI, and PVA+APS+MB+PANI were constructed. The electrochromic devices were approximately 2 in.×2 in. in width and length. The gels were enabled to settle and dry before the experiments were performed. In some cases, the edges of the electrochromic devices were sealed using Loctile super-glue.

FIGS. 2A and 2B are photographs of an example single active layer electrochromic device that was fabricated. The active layer comprised a gel mixture of PVA+APSMB+PANI. When 2 V was applied to the active layer, a substantially opaque state shown in FIG. 2A resulted. When the electrical potential of the gel was reduced to −0.5 V, a substantially transparent state shown in FIG. 2B resulted. As can be appreciated from FIG. 2B, the gel is not merely translucent as the color is so light that detailed images could be seen through the gel.

FIGS. 3A-3C are scanning electron microscope (SEM) images of three different active layer gels, including PVA+APS+MB, PVA+APS+PANI, and PVA+APS+MB+PANI, respectively that were formed on FTO-coated glass and dried at room temperature. The surface properties of the gels are important to understand the mechanism of color change in the active layer. FIGS. 3A and 3B show typical compact symmetric structure with packed pebble-like structure. A small amount of methylene blue dye added to the PVA+APS+MB+PANI active layer produced a fibrillar structure (FIG. 3C).

FIG. 4 shows Fourier-transform infrared spectroscopy (FTIR) transmission peaks at 3416 nm (stretching vibration O—H with strong hydrogen bonding intermolecular and intramolecular types), 2953 cm⁻¹ (to C—H alkyl group), 2345 cm⁻¹, 2099 cm⁻¹, 1737 cm⁻¹ (C═O), 1650 cm⁻¹ (C═O stretching), 1409 cm⁻¹ (C—H₂), 1206 cm⁻¹ (C—N stretching of amine), 1105 cm⁻¹ (is due to S═O), and 820 cm⁻¹ (C—S bond) for a PVA+APS gel. The characteristics peaks of PVA+APS gel at 3420 cm⁻¹, 2927 cm⁻¹, 2156 cm⁻¹, 1645 cm⁻¹, 1418 cm⁻¹, 1221 cm⁻¹, 1090 cm⁻¹, 839 cm⁻¹, and 593 cm⁻¹ with little were observed due to presence of methylene blue in Curve 2. The peak 1409 cm⁻¹ has been shifted to 1418 cm⁻¹ due to the presence of methylene blue. The characteristic peaks of methylene blue at 1595 cm⁻¹, 1487 cm⁻¹, 1390 cm⁻¹ as well as 816 cm⁻¹ were not observed. Instead, the characteristic peaks shifted due to the presence of methylene blue in PVA+APS+MB gel, as shown in Curve 2. The presence of polyaniline in PVA+APS+PANI+MB resulted in transmission peaks at 3445 cm⁻¹ (v(N—H) (stretching vibrations), 3222 cm⁻¹ (H-bonded v(N—H), 2948 cm⁻¹, 2601 cm⁻¹, 1645 cm⁻¹ (1486 benzenoid ring stretching), 1418 cm⁻¹ (phenyl ring stretching), 1312 cm⁻¹ (ν(C—N.⁺), 1211 cm⁻¹ (ν(C—N), 1109 cm⁻¹ (B—NH—B/δ(C—H), 728 cm⁻¹ (c(C—H) (monosubstituted or 1,2-disubstituted ring), 685 cm⁻¹ (out-of-plane ring bending (monosubstituted ring)), 598 cm⁻¹ (Cl−), and 482 cm⁻¹, as shown in Curve 3. The peak at 1109 cm⁻¹ is associated with charged polymer units quinoid (Q)=NH+− benzene B or (B)—NH⁺.—B. PVA+APS+PANI+MB had FTIR transmission peaks at 3416 cm⁻¹, 3213 cm⁻¹, 2943 cm⁻¹, 2601 cm⁻¹, 2108 cm⁻¹, 1640 cm⁻¹, 1491 cm⁻¹, 1408 cm⁻¹, 1283 cm⁻¹, 1201 cm⁻¹, 1098 cm⁻¹, 820 cm⁻¹, 733 cm⁻¹, 675 cm⁻¹, 612 cm⁻¹, 521 cm⁻¹, and 477 cm⁻¹, as shown in Curve 4. The peaks were due to the presence of polyvinyl alcohol, methylene blue, and polyaniline in doped states.

Curve 1 in FIG. 5 reveals UV-vis optical absorption at 381 nm, 673 nm, and 764 nm of PVA+APS gel coated on glass plate and dried at room temperature. Curve 2 shows the UV-vis absorption at 405 nm, 623 nm, 679 nm, 739 nm, and 753 nm for PVA+HCl+APS+MB based gel deposited on glass substrate. Curve 3 shows UV-vis absorption peaks at 386 nm, 427 nm, and 820 nm for PVA+APS+PANI+MB. However, the absorption peaks at 405 nm, 626 nm, 680 nm, 739 nm, and 757 nm were observed for PVA+APS+PANI+MB electrolyte on glass plate. The presence of a peak at 820 nm in Curve 3 and 757 nm in Curve 4 of FIG. 5 are indicative of the doped state of polyaniline regardless of the presence of ammonium perdisulphate oxidant.

Electrochromic devices were fabricated by applying a layer of the gel between two FTO-coated glass plates for the purpose of studying the electrochromic response of the gels. The fabricated devices were tested by applying electrical potentials to the conductive glass plates. FIG. 6A shows cyclic voltammetries (CVs) of a PVA+APS+MB device as a function of the scan rate. The CVs show oxidation peaks varying from 1.49 V to 1.42 V, whereas the reduction peaks from the four different scan rates were observed at ˜1.48 V, ˜0.73 V, and ˜−0.13 V. A dark blue color change was observed at around 1.45 V depending upon the scan potential. However, a substantially transparent color was observed for the potential around −0.2 V. The complete reversibility in coloration of PVA+APS+MB device was found between the potential range of 2.0 V to −0.5 V.

FIG. 6B shows CVs of a PVA+APS+PANI device. A broad oxidation peak can be observed at 1.30 V to 1.69 V, and a small peak can be observed at 1.37 V to 1.67 V. A reduction peak occurred at 0.47 V and 0.8 V as a function of scan rate.

FIG. 6C shows the CVs of PVA+APS+PANI+MB. The range of redox potential changed as a function of scan rate. The increase in current is proportional to scan rate and the process was diffusion controlled. However, there was a shift in the oxidation potential at ˜1.4 V for the scan rate of 50 mV/sec and 100 mV/sec indicating that the redox materials in the layer are not confined to the surface electrodes at scans at higher potentials. The reversibility in the CVs shows that the reaction is a diffusion process. However, the shift in the redox peak potential is a contribution from migration and adsorption effects besides diffusion control.

FIGS. 7A-7D shows the CVs of PVA+APS+PANI+MB devices at 50 mV/sec, where the gel was formed by keeping various molar ratios of aniline to methylene blue at 1:2.0, 1:2.5, 1:3, and 1:5, respectively. The gel containing a methylene blude to analine ratio of 1:2.5 to 1:3.0 has better color contrast and a faster switching response (100 ms). The redox potential for the PVA+APS+PANI+MB device exhibited a sharp oxidation peak at around 1.42 V and a reduction peak at around −0.5 V. However, the reduction peak occurred at 0.06 V, which shows transition in the color change from dark blue to green and further, faded yellow or transparent by approaching at −0.5 V.

FIGS. 8A-8C show chronoamperometric results of PVA+APS+PANI, PVA+APS+MB, and PVA+APS+MB+PANI in a single active layer between two FTO-coated glass plates. FIG. 8A shows chronoamperometric results for the PVA+APS+PANI layer, indicating that the reduction current is larger than the oxidation of the electrolyte. The chronoamperometric study was performed by applying a pulse between the two oxidation and reduction potentials. However, no biasing current was applied to compensate the self-erasing reactions. The potential was applied at 1.5 V and immediately changed to −0.5 V. The colored state remained at 1.5 V and application of −0.5 V showed the reduction state of the layer. When the applied 1.5 V was switched off, the dark blue color lasted for a long time. Similarly, when the applied −0.5 V was switched off, a nearly transparent color lasted for several hours. That the dark- and light-colored states remained after cutting of the applied potential is indicative of the potential as a window for the single active layer electrochromic device. FIG. 8B shows the redox process of PVA+APS+MB for a single active layer electrochromic device. As shown in FIG. 8C, the redox processes for PVA+APS+PANI+MB are asymmetric, similar to PVA+APS+PANI. The polyaniline and methylene blue present in the PVA+APS+PANI+MB contributes to faster coloration and decoloration as compared to polyaniline and methylene blue present in the PVA+APS device.

The mechanism of gelling of the active layer will now be discussed. The polyvinyl alcohol gelling depends on the condensation reaction and temperature applied to the polyvinyl alcohol in a hydrogen chloride (HCl) solution. The water molecules are released and chlorine atoms of the HCl attach to the polyvinyl alcohol in the gelling process. FIG. 10 illustrates the gelling process of polyvinyl alcohol in an HCl solution.

Adding ammonium perdisulphate oxidant to the polyvinyl alcohol gel causes the loss of electrons from the structure. This process produces the lone-pair effect in the carbon structure, as shown in FIG. 11.

Adding aniline to PVA+APS causes oxidative polymerization and forms the emeraldine salt (ES) form of polyaniline. The possible interaction of emeraldine salt with PVA+APS gel forms a PVA+APS+PANI structure. The emeraldine salt state interacts with chlorine atoms in PVA+APS gel due to lone-pair effect of the emeraldine salt state of polyaniline, as shown in FIG. 12. However, the presence of ammonium perdisulphate causes the oxidation of the emeraldine salt state and forms a pernigraniline state (purple or dark blue in color) of polyaniline (based on UV-vis measurement and optical observation).

FIG. 13 illustrates the possible interaction of methylene blue with the PVA+APS+PANI structure. There is a weak bond that is established between the nitrogen of methylene blue to hydrogen-bonded with nitrogen present in polyaniline structure. The application of a voltage to the PVA+APS+MB+PANI device produces a color change from blue to transparent or faded yellow. The oxidation of methylene blue and polyaniline produces a dark blue color in the PVA+APS+MB+PANI device, as shown in FIG. 14. The color changes from dark blue to substantially transparent by applying a potential varying from a range of −0.5 V to 0 V to a range of 1.5 V to 2 V. However, the maximum −0.5 V potential brings about a transparent state faster. To achieve the electrochromic behavior in a single layer, the electron donor and electron acceptor must be present in the structure.

Interestingly, the electrochromic device has been achieved with MB+APS+PVA, PVA+APS+PANI, as well as PVA+APS+MB+PANI gels. The color contrast, potential window, stability of gel, and the reversibility of the device are dependent of the type of gel. The PVA+APS+MB gel showed state reversibility for nearly 100 to 200 cycles, whereas the PVA+APS+PANI gel did not have better color contrast. However, PVA+APS+MB+PANI gel operated through greater than 1000 cycles with no decay and had better color contrast with 60% transparency. The application of a gel is simple and it can be easily applied, thereby eliminating the need for any complicated vacuum process, such as sputtering, ion-beam, etc.

In summary, the disclosed electrochromic devices are unique in that they comprise a single active layer that includes a base polymer, an acid, an oxidant, and a conducting polymer, dye, or both. The range of potential for transparency (or substantial transparency) is between approximately −0.5 V to 0 V and a dark color (e.g., dark blue) is observed in the range of approximately 1.5 V to 2.0 V. The single active layer electrochromic devices can be easily applied to window applications as well as goggle application without involving complicated fabrication processes, which are common for conventional electrochromic devices. The single active layer electrochromic devices can further be integrated with small solar cells that can generate the voltages required to darken the device for energy saving applications. 

The invention claimed is:
 1. A method for controlling transmission of light, the method comprising: applying an electrical potential to a predetermined active layer of an electrochromic device to cause the electrochromic device to enter a light-blocking state in which the predetermined active layer is opaque, wherein the predetermined active layer comprises a base polymer, an acid, an oxidant, and a colored material; and reversing the electrical potential applied to the predetermined active layer to cause the device to enter a light-transmitting state in which the predetermined active layer is substantially transparent; wherein the device comprises no other active layer other than the predetermined active layer that contribute to transitioning between the light-blocking state and the light-transmitting state.
 2. The method of claim 1, wherein said applying an electrical potential comprises applying approximately 1.5 V to 2.0 V to the predetermined active layer.
 3. The method of claim 2, wherein said reversing the electrical potential comprises reducing the electrical potential applied to the predetermined active layer to approximately 0 V to −0.5 V.
 4. The method of claim 1, wherein said applying includes applying the electrical potential to the predetermined active layer sandwiched between first and second transparent or translucent layers of material.
 5. The method of claim 1, wherein said applying includes applying the electrical potential to the predetermined active layer comprising a dye.
 6. The method of claim 1, wherein said applying includes applying the electrical potential to the predetermined active layer comprising a conducting polymer.
 7. The method of claim 6, wherein said applying includes applying the electrical potential to the predetermined active layer comprising one or more of polyvinyl alcohol (PVA), poly (vinyl acetate), poly (vinyl alcohol co-vinyl acetate), polyvinyl acetate-vinyl alcohol, poly (methyl methacrylate, poly (vinyl alcohol-co-ethylene ethylene), poly (vinyl butyral-co-vinyl alcohol-co-vinyl acetate), poly(vinyl alcohol)-acrylamide, polyvinyl butyral, polyvinyl chloride, poly(vinyl nitrate), substituted (butyryl, palmitic, capryloyl, lauric, myristic, and stearic acids, myristol, halogens, azide, or amines, poly(vinyl alcohol), carboxylated poly(vinyl alcohol), poly(vinyl chloride-co-vinyl acetate-co-vinyl alcohol), poly(vinyl acetate-co-acrylic acid), poly(vinyl alcohol-co-acrylic acid), poly(vinyl alcohol)-acrylamide, poly(vinyl alcohol)-salicylic acid, poly(vinyl methyl ketone), and a mixture thereof. 